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2,3-dichloro-5,8-dihydroxy-1,4-naphthoquinone | 38572-68-8

中文名称
——
中文别名
——
英文名称
2,3-dichloro-5,8-dihydroxy-1,4-naphthoquinone
英文别名
2,3-Dichloronaphthazarin;6,7-dichloro-5,8-dihydroxynaphthalene-1,4-dione
2,3-dichloro-5,8-dihydroxy-1,4-naphthoquinone化学式
CAS
38572-68-8
化学式
C10H4Cl2O4
mdl
——
分子量
259.045
InChiKey
KFAVXUQFBGHURZ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    540.4±50.0 °C(Predicted)
  • 密度:
    1.807±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Metallacycles and methods of making the same
    申请人:Lu Kuang-Lieh
    公开号:US20090082574A1
    公开(公告)日:2009-03-26
    The present invention provides for novel metallacycles and processes for making the same.
    本发明提供了一种新型属环化合物和制备方法。
  • An Experimental and Density Functional Theory Approach Towards the Establishment of Preferential Metal‐ or Ligand‐Based Electron‐Transfer Processes in Large Quinonoid‐Bridged Diruthenium Complexes [{(aap) <sub>2</sub> Ru} <sub>2</sub> (μ‐BL <sup> 2 <i>–</i> </sup> )] <sup> <i>n</i> + </sup> (aap = 2‐Arylazopyridine)
    作者:Sandeep Ghumaan、Sriparna Mukherjee、Sanjib Kar、Dipankar Roy、Shaikh M. Mobin、Raghavan B. Sunoj、Goutam Kumar Lahiri
    DOI:10.1002/ejic.200600638
    日期:2006.11
    class II mixed-valence system. Electrogenerated EPR-inactive second-step oxidized species [1–8] 4+ have been described as spin-coupled radical-bridged mixed-valence ruthenium (II)(III) species, Ru II (π-BL – )Ru III }. [1–8] 2+ exhibit multiple ligand-based reductions involving coordinated BL 2– as well as aap. The above preferential metal- or ligand-based accessible electron-transfer processes in the
    一组十个醌型桥连二(II)配合物[(aap) 2 Ru II (μ-BL 1 2– )Ru II (aap) 2 ](ClO 4 ) 2 , [1a–1c](ClO 4 ) 2 [(pap) 2 Ru II (μ-BL n 2– )Ru II (pap) 2 ](ClO 4 ) 2 [2–8](ClO 4 ) 2 [aap = 2-芳基并吡啶,NC 5 H 4 – N = N–C 6 H 4 (R) R = H (pap) [1a](ClO 4 ) 2 , m-Me [1b](ClO 4 ) 2 , m-Cl [1c](ClO 4 ) 2 }; BL 2– = 5,8-dioxido-1,4-napthoquinone (BL 1 2– ), 2,3-dichloro-5,8-dioxido-1,4-napthoquinone (BL 2 2– ), 6,11-二化-5,12-
  • Chemistry of naphthazarin derivatives: XV. Bromination of naphthazarin and its derivatives
    作者:N. D. Pokhilo、A. Ya. Yakubovskaya、V. P. Glazunov
    DOI:10.1134/s1070428011040063
    日期:2011.4
    Bromination of a number of naphthazarin (5,8-dihydroxy-1,4-naphthoquinone) derivatives having different substituents in the aromatic ring with molecular bromine in carbon tetrachloride was studied. Preparative procedures for the synthesis of 2-bromo-5,8-dihydroxy-7-methoxy-1,4-naphthoquinone, 2-bromo-6,7-dichloro-5,8-dihydroxy-1,4-naphthoquinone, 2-bromo-3,5,8-trihydroxy-1,4-naphthoquinone, and 2-bromo-6
    研究了在四氯化碳中用分子化许多在芳环上具有不同取代基的沙林(5,8-二羟基-1,4-萘醌)衍生物的方法。合成2--5,8-二羟基-7-甲基-1,4-萘醌,2--6,7-二-5,8-二羟基-1,4-萘醌,2-的制备方法开发了3,5,8-三羟基-1,4-萘醌和2--6,7-二-3,5,8-三羟基-1,4-萘醌
  • NOVEL SYNTHESES OF PHENOSELENAZINEQUINONE INFRARED DYES
    作者:Sung Hoon Kim、Masaru Matsuoka、Teijiro Kitao
    DOI:10.1246/cl.1985.1351
    日期:1985.9.5
    New series of phenoselenazinequinone infrared dyes for optical recording medium have been synthesized by the ring-closure reaction between 2,3-dihalogenoquinones and zinc 2-aminobenzeneselenate. These dyes absorbed near infrared light at 700–830 nm.
    通过2,3-二卤代醌与2-硒酸的闭环反应合成了一系列用于光记录介质的新型吩嗪醌红外染料。这些染料吸收 700-830 nm 的近红外光。
  • MATSUOKA, MASARU;HAMANO, KATSUHISA;KITAO, TEIJIRO, SYNTHESIS, BRD, 1984, N 11, 953-955
    作者:MATSUOKA, MASARU、HAMANO, KATSUHISA、KITAO, TEIJIRO
    DOI:——
    日期:——
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